About this trial
This study aims to investigate the value of 18F-FDG\&68Ga-FAPI PET/CT in evaluating the outcome of conversion therapy and the prognosis of people with peritoneal metastases from gastric cancer.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Histologically confirmed gastric adenocarcinoma with no history of resection of primary or metastatic lesions
Peritoneal metastases of gastric cancer requiring laparoscopy for definitive diagnosis without gastric outflow tract obstruction and intestinal obstruction
Patients voluntarily enrolled in this study by signing an informed consent form
Age ≥ 18 years
Disqualifiers
Signs of distant metastases other than peritoneal metastases at enrolment
Pregnant or breastfeeding women.
Patients with a history of other malignant diseases in the last 5 years, except cured skin cancer and carcinoma in situ of cervix
Severe mental disease, uncontrolled epilepsy, or central nervous system disease
Trial population
Eligible inpatients and outpatients from Ruijin Hospital
Trial design
Other
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Target-to-background ratio(TBR)
68Ga-FAPI and 18F-FDG uptake ratio of primary gastric lesions, peritoneal lesions and recurrent metastatic lesions to mediastinum and liver blood pool on PET/CT images.
Standardized uptake value(SUV)
SUV of 68Ga-FAPI and 18F-FDG uptake on PET/CT images for primary gastric lesions, peritoneal lesions and recurrent metastatic lesions
Evaluation the outcome of conversion therapy
The value of 68Ga-FAPI PET/CT and 18F-FDG PET/CT in evaluating the outcome of conversion therapy in gastric cancer with peritoneal metastasis.
Secondary outcomes
Progress free survival
Progress free survival
Overall survival
Overall survival
Sponsors and contacts
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